Pharmaceutical 99% Purity Metallothionein Powder Material Metallothionein Mt Rabbit Liver Zinc Metallothionein
Model NO.
D-sung Metallothionein
Test Method
HPLC
Shelf Life
2 Years
Specific
COA
Application
Pharmaceutical
MW
0
Storage
Normal
Mf
C222h379 N71 O84 S21
CAS No.
73767-16-5
Form
Powder
Color
White
Name
Metallothionein Powder
Assay
HPLC 99%
Grade
Pharmaceutical Grade
Transport Package
Negotiable
Specification
99%
Trademark
D-sung
Origin
Shaanxi Xi′an
Production Capacity
500kg/Month
Reference Price
$ 81.00 - 135.00
Description
Product Description
Pharmaceutical
99%
Purity Metallothionein powder Material Metallothionein Mt
Rabbit Liver Zinc Metallothionein
| Product name | Metallothionein |
| Cas number | 73767-16-5 |
| Appearance | White powder |
| MF | C222H379 N71 O84 S21 |
| MW | 0 |
Metallothionein is a low molecular weight protein with metal binding ability and high induction properties. [1] Short peptides rich in cysteine with high affinity for a variety of heavy metals. It is a protein with low molecular weight and extremely high content of cysteine residues and metals. The combined metals are mainly cadmium, copper and zinc, which are widely present in various organisms from microorganisms to humans, and their structure is highly conserved.
Heavy metal detoxification function
MT is a metal-binding protein rich in cysteine. Its sulfhydryl group can strongly chelate toxic metals and excrete them from the body, thereby achieving detoxification. [4] MT is related to the metabolism of trace metals. In all mammalian tissues, MT-1 and MT-2 are expressed synergistically. MT-3 is a specific member of the brain in this family. It can bind zinc and copper and has important neurophysiological and neuromodulation functions. Studies on many aquatic organisms have shown that MT plays an important role in the regulation of basic metal elements, and has inhibitory and detoxifying effects on non-basic metal elements. MT can effectively reduce the toxicity of heavy metals to the body by combining with heavy metals, and it is currently the most ideal biological chelating antidote in clinical practice.
Environmental protection
Utilizing the characteristics of the combination of MT and metal, it is possible to breed or use genetic engineering to establish a high expression system of MT to control heavy metal pollution. According to reports, tobacco transfected with yeast MT gene can significantly increase the absorption of cu2 in contaminated soil, and this method can be used to remedy areas contaminated by heavy metals.
MT and radiation resistance
Ionizing radiation can produce a large amount of free radicals, which can damage organisms directly or indirectly. Studies have shown that oral administration of MT can prolong the survival time of mice exposed to a one-time high-dose ionizing radiation, and reduce the damage to the immune system caused by one-time high-dose and multiple low-dose ionizing radiation. Oral MT can absorb a large amount of Cys that enters the body. It provides raw materials for repairing the disulfide bonds broken by radiation in the body.
MT and Parkison (PD) disease
Many experiments have proved that MT has a protective effect on the nervous system. Experiments have shown that in transgenic mice, overexpression of MT-1 can change the symptoms of encephalitis and promote brain repair. It is a protective factor in nerve cells. Through the study of rat stabbing model and ischemia model, it is found that MT-3 is involved in the repair of central nervous system damage. PD disease is caused by the induction of free radicals by 6-hydroxydopamine, and certain inducers of MT isoforms in the brain, such as oxidative stress, cytokines and inflammatory processes, can prevent this neurotoxicity, which is free from MT clearance Base related.
Heavy metal detoxification function
MT is a metal-binding protein rich in cysteine. Its sulfhydryl group can strongly chelate toxic metals and excrete them from the body, thereby achieving detoxification. [4] MT is related to the metabolism of trace metals. In all mammalian tissues, MT-1 and MT-2 are expressed synergistically. MT-3 is a specific member of the brain in this family. It can bind zinc and copper and has important neurophysiological and neuromodulation functions. Studies on many aquatic organisms have shown that MT plays an important role in the regulation of basic metal elements, and has inhibitory and detoxifying effects on non-basic metal elements. MT can effectively reduce the toxicity of heavy metals to the body by combining with heavy metals, and it is currently the most ideal biological chelating antidote in clinical practice.
Environmental protection
Utilizing the characteristics of the combination of MT and metal, it is possible to breed or use genetic engineering to establish a high expression system of MT to control heavy metal pollution. According to reports, tobacco transfected with yeast MT gene can significantly increase the absorption of cu2 in contaminated soil, and this method can be used to remedy areas contaminated by heavy metals.
MT and radiation resistance
Ionizing radiation can produce a large amount of free radicals, which can damage organisms directly or indirectly. Studies have shown that oral administration of MT can prolong the survival time of mice exposed to a one-time high-dose ionizing radiation, and reduce the damage to the immune system caused by one-time high-dose and multiple low-dose ionizing radiation. Oral MT can absorb a large amount of Cys that enters the body. It provides raw materials for repairing the disulfide bonds broken by radiation in the body.
MT and Parkison (PD) disease
Many experiments have proved that MT has a protective effect on the nervous system. Experiments have shown that in transgenic mice, overexpression of MT-1 can change the symptoms of encephalitis and promote brain repair. It is a protective factor in nerve cells. Through the study of rat stabbing model and ischemia model, it is found that MT-3 is involved in the repair of central nervous system damage. PD disease is caused by the induction of free radicals by 6-hydroxydopamine, and certain inducers of MT isoforms in the brain, such as oxidative stress, cytokines and inflammatory processes, can prevent this neurotoxicity, which is free from MT clearance Base related.
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